In patients with PKD, kidneys may keep functioning well for some time, even if they are enlarged with cysts. Tracking your kidney size, or total kidney volume (TKV) can help your doctor predict how quickly may progress for you over time.

How does IgA Nephropathy (IgAN) affect people in different parts of the world?  How common is IgAN from the North America to Africa to Asia?

IgA Nephropathy (IgAN) is an autoimmune disease that can lead to inflammation and damage to the filtering units of the kidneys.  It is estimated that 20-40% of affected individuals will develop kidney failure.

When you are caring for someone with autosomal dominant polycystic kidney disease (ADPKD), it may be difficult to focus on your needs as well as those of your loved one.

Because ADPKD is genetic, meaning it runs in families, it can affect the family as a whole. This is one reason you may find it essential to talk with family about your diagnosis.

ADPKD, or autosomal dominant polycystic kidney disease, accounts for most cases of polycystic kidney disease (9 out of 10). Some people with ADPKD are at risk for accelerated disease progression.